Progestin stimulated extracellular matrix formation in immortalized human leiomyoma two-dimensional and three-dimensional cultures, and mifepristone inhibited progestin-stimulated extracellular matrix protein components involved in aberrant fibrosis.
This study demonstrates for the first time that oocytes with normal spindle morphology are more likely to produce euploid embryos compared with oocytes with translucent or no visible meiotic spindles.
Poor expression of implantation markers and altered leukemia inhibitory factor–signal transducers and activators of transcription 3 (LIF-STAT3) signaling in women with dormant genital tuberculosis is associated with implantation failure. Alterations in LIF-STAT3 signaling in heat shock protein-65-treated human endometrial stromal cells confirms compromised endometrial decidualization.
Epidermal growth factor–containing fibulin-like extracellular matrix protein 1 gene expression and fibulin- 3 protein expression are significantly down-regulated in leiomyomas versus myometrium in vivo and in vitro. Differences in expression are partially due to differences in methylation status.
The performance of the different commercial antimullerian hormone assays for polycystic ovary syndrome diagnosis is comparable, but different threshold values should be used for automatic and manual assays.
Oral administration of an FSH agonist demonstrated acceptable exposure and was well tolerated. No clear effect was observed on follicular development; higher doses were not tested owing to thyroid function test changes.
Next-generation sequencing allows for the detection of pure and mosaic segmental aneuploidies with the same efficiency as array comparative genomic hybridization.
In female balanced X-autosome translocation, normal/balanced female embryos obtained after a preimplantation genetic diagnosis procedure and transferred have a potential risk of clinical abnormalities owing to the uncertain outcome of X inactivation.
Consumption of a Western-style diet by female nonhuman primates with and without mildly elevated testosterone alters small antral follicle morphology, numbers, health, and RNA transcriptome.
Women who conceived with fertility treatments were more likely to stop breast feeding and provide formula to their infants earlier. A higher prevalence of preterm birth does not fully explain these associations.
Children from oocytes and embryos infected with hepatitis B virus (HBV) were not chronically infected after birth; the HBsAg in oocytes and embryos may not result in vertical transmission.
In 807,765 singleton pregnancies in Ontario, Canada, the risk of placental complications was sixfold higher in hypertensive women using assisted reproduction technology compared with normotensive women in unassisted pregnancies.
Women with endometriosis, in addition to genetic predisposition, are exposed more frequently to preterm birth during intrauterine life and to formula feeding in early postnatal life.
Our study showed that, in Caucasian women, genetic variants in the PLGF rs2268613 gene influences PLGF plasma levels. Plasma levels of VEGF were elevated in endometriosis patients compared with controls.
Assisted reproduction technology has no adverse impact on pain symptoms or quality of life in women with endometriosis of any phenotype as compared with healthy women.
Excising endometriotic lesions significantly decreased circulating levels of inflammatory cytokines. Levels were also higher than in normal women, dissimilar in eutopic versus ectopic endometrium, and influenced by disease stage.
Cesarean scar pregnancies are challenging to diagnose and treat owing to the heterogenic appearance and treatment possibilities. This systematic review supports an interventional rather than medical approach.
Lower and higher antimullerian hormone levels are not associated with human chorionic gonadotropin- detected or clinical pregnancy loss in unassisted conceptions in women with a history of pregnancy loss.
We and selected partners, use cookies or similar technologies as specified in the cookie policy and privacy policy.
You can consent to the use of such technologies by closing this notice.
Cookie Control
Customise your preferences for any tracking technology
The following allows you to customize your consent preferences for any tracking technology used
to help us achieve the features and activities described below. To learn more about how these trackers help us
and how they work, refer to the cookie policy. You may review and change your preferences at any time.
These trackers are used for activities that are strictly necessary to operate or deliver the service you requested from us and, therefore, do not require you to consent.
These trackers help us to provide a personalized user experience by improving the quality of your preference management options, and by enabling the interaction with external networks and platforms.